Colon Cancer: Gene >> CNTD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000430325
Start	40223116:40223116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777209195
CDS Mutation	c.860G>A
AA Mutation	p.Arg287His(p.R287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000430325
Start	40223098:40223098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878C>T
AA Mutation	p.Pro293Leu(p.P293L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430325
Start	40224803:40224803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430325
Start	40226603:40226603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CNTD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000430325
Start	40223144:40223144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832C>A
AA Mutation	p.Leu278Ile(p.L278I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript